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IMPROvER: the Integral Membrane Protein Stability Selector.
Harborne, Steven P D; Strauss, Jannik; Boakes, Jessica C; Wright, Danielle L; Henderson, James G; Boivineau, Jacques; Jaakola, Veli-Pekka; Goldman, Adrian.
Afiliação
  • Harborne SPD; Astbury Centre for Structural and Molecular Biology, University of Leeds, Leeds, UK. steven.harborne@peakproteins.com.
  • Strauss J; Peak Proteins, BioHub, Alderley Park, Macclesfield, UK. steven.harborne@peakproteins.com.
  • Boakes JC; Astbury Centre for Structural and Molecular Biology, University of Leeds, Leeds, UK.
  • Wright DL; Astbury Centre for Structural and Molecular Biology, University of Leeds, Leeds, UK.
  • Henderson JG; Astbury Centre for Structural and Molecular Biology, University of Leeds, Leeds, UK.
  • Boivineau J; Astbury Centre for Structural and Molecular Biology, University of Leeds, Leeds, UK.
  • Jaakola VP; Novartis Institutes for Biomedical Research, Chemical Biology and Therapeutics, Virchow 16, Basel, Switzerland.
  • Goldman A; Confo Therapeutics, Technologiepark 94, 9052, Zwijnaarde, Belgium.
Sci Rep ; 10(1): 15165, 2020 09 16.
Article em En | MEDLINE | ID: mdl-32938971
ABSTRACT
Identifying stabilising variants of membrane protein targets is often required for structure determination. Our new computational pipeline, the Integral Membrane Protein Stability Selector (IMPROvER) provides a rational approach to variant selection by employing three independent approaches deep-sequence, model-based and data-driven. In silico tests using known stability data, and in vitro tests using three membrane protein targets with 7, 11 and 16 transmembrane helices provided measures of success. In vitro, individual approaches alone all identified stabilising variants at a rate better than expected by random selection. Low numbers of overlapping predictions between approaches meant a greater success rate was achieved (fourfold better than random) when approaches were combined and selections restricted to the highest ranked sites. The mix of information IMPROvER uses can be extracted for any helical membrane protein. We have developed the first general-purpose tool for selecting stabilising variants of [Formula see text]-helical membrane proteins, increasing efficiency and reducing workload. IMPROvER can be accessed at http//improver.ddns.net/IMPROvER/ .
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Engenharia de Proteínas / Estabilidade Proteica / Proteínas de Membrana Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Engenharia de Proteínas / Estabilidade Proteica / Proteínas de Membrana Idioma: En Ano de publicação: 2020 Tipo de documento: Article